Canonical Allele Identifier: CA366234211

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510880C>T (hg19) ; chr6:g.157189746C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189746C>T , CM000668.2:g.157189746C>T	GRCh38
NC_000006.11:g.157510880C>T , CM000668.1:g.157510880C>T	GRCh37
NC_000006.10:g.157552572C>T	NCBI36
NG_032093.1:g.416817C>T
NG_032093.2:g.416817C>T
NG_066624.1:g.418721C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3865C>T	ENSP00000055163.8:p.Pro1289Ser
ENST00000414678.8:c.3934C>T	ENSP00000412835.3:p.Pro1312Ser
ENST00000637015.2:c.4153C>T	ENSP00000489729.2:p.Pro1385Ser
ENST00000346085.10:c.3904C>T	ENSP00000344546.5:p.Pro1302Ser
ENST00000350026.10:c.3616C>T	ENSP00000055163.7:p.Pro1206Ser
ENST00000414678.7:c.2182C>T	ENSP00000412835.2:p.Pro728Ser
ENST00000635849.1:c.1345C>T	ENSP00000490948.1:p.Pro449Ser
ENST00000635957.1:c.979C>T	ENSP00000490385.1:p.Pro327Ser
ENST00000636930.2:c.4024C>T MANE Select	ENSP00000490491.2:p.Pro1342Ser
ENST00000636940.1:n.2021C>T
ENST00000637015.1:c.1392C>T
ENST00000637568.1:c.1306C>T
ENST00000637741.1:n.690C>T
ENST00000637810.1:c.1366C>T	ENSP00000489636.1:p.Pro456Ser
ENST00000637904.1:c.1525C>T	ENSP00000490550.1:p.Pro509Ser
ENST00000647938.1:c.3655C>T	ENSP00000498155.1:p.Pro1219Ser
ENST00000346085.9:c.3655C>T	ENSP00000344546.4:p.Pro1219Ser
ENST00000350026.9:c.3616C>T	ENSP00000055163.7:p.Pro1206Ser
ENST00000414678.6:c.2182C>T	ENSP00000412835.2:p.Pro728Ser
NM_017519.2:c.3616C>T	NP_059989.2:p.Pro1206Ser
NM_020732.3:c.3655C>T	NP_065783.3:p.Pro1219Ser
XM_005267069.3:c.3775C>T	XP_005267126.2:p.Pro1259Ser
XM_011535984.1:c.2854C>T	XP_011534286.1:p.Pro952Ser
XM_011535985.1:c.2674C>T	XP_011534287.1:p.Pro892Ser
XM_011535986.1:c.2434C>T	XP_011534288.1:p.Pro812Ser
XM_011535987.1:c.2053C>T	XP_011534289.1:p.Pro685Ser
XM_011535988.1:c.916C>T	XP_011534290.1:p.Pro306Ser
NM_001346813.1:c.3775C>T	NP_001333742.1:p.Pro1259Ser
NM_001363725.1:c.1525C>T	NP_001350654.1:p.Pro509Ser
XM_011535984.2:c.3985C>T	XP_011534286.2:p.Pro1329Ser
XM_011535988.3:c.916C>T	XP_011534290.1:p.Pro306Ser
XM_017011103.2:c.3886C>T	XP_016866592.1:p.Pro1296Ser
XM_017011104.1:c.3856C>T	XP_016866593.1:p.Pro1286Ser
XM_017011105.2:c.3826C>T	XP_016866594.1:p.Pro1276Ser
XM_017011106.2:c.3697C>T	XP_016866595.1:p.Pro1233Ser
XM_017011107.2:c.3676C>T	XP_016866596.1:p.Pro1226Ser
XR_002956289.1:n.4068C>T
NM_001363725.2:c.1525C>T	NP_001350654.1:p.Pro509Ser
NM_001371656.1:c.3904C>T	NP_001358585.1:p.Pro1302Ser
NM_001374820.1:c.3904C>T	NP_001361749.1:p.Pro1302Ser
NM_001374828.1:c.4024C>T MANE Select	NP_001361757.1:p.Pro1342Ser
NM_017519.3:c.3865C>T	NP_059989.3:p.Pro1289Ser